Evidence map›Paper›PMID 30929401›Full record

ArticleJournal of clinical research in pediatric endocrinology2020

Hypophosphatasia: A Novel Mutation Associated with an Atypical Newborn Presentation

Roger Esmel-Vilomara, Susana Hernández, Ariadna Campos-Martorell, Eva González-Roca, Diego Yeste, Félix Castillo

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Hypophosphatasia: The Unusual PresentationJournal of clinical research in pediatric endocrinology · 2020
    Article
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Roger Esmel-VilomaraHospital Universitari Vall d’Hebron, Clinic of Pediatrics, Barcelona, SpainORCID 0000-0003-4449-3217
Susana HernándezHospital Universitari Vall d’Hebron, Clinic of Neonatology, Barcelona, SpainORCID 0000-0001-5809-7763
Ariadna Campos-MartorellHospital Universitari Vall d’Hebron, Clinic of Pediatric Endocrinology, Barcelona, SpainORCID 0000-0002-8134-4934
Eva González-RocaHospital Clínic de Barcelona, Clinic of Immunology, Barcelona, SpainORCID 0000-0002-1126-0321
Diego YesteHospital Universitari Vall d’Hebron, Clinic of Pediatric Endocrinology, Barcelona, SpainORCID 0000-0002-6620-6525
Félix CastilloHospital Universitari Vall d’Hebron, Clinic of Neonatology, Barcelona, SpainORCID 0000-0003-3155-6290
Vall d'Hebron Hospital Universitari · ESHospital Clínic de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypophosphatasia, a rare genetic disease affecting bone metabolism, is characterized by decreased activity of tissue non-specific alkaline phosphatase (TNAP). The gene encoding TNAP

Indexed as

Alkaline PhosphataseHumansHypophosphatasiaInfant, NewbornInfant, PrematureMaleMutationPhenotypeAlkaline PhosphataseALPL protein, humanalkaline phosphataseHypophosphatasiamutationnewborn

Identifiers

PMID30929401
PMCPMC7127881
OpenAlexW2934305444

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.